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Journal ArticleDOI

The codon 72 polymorphic variants of p53 have markedly different apoptotic potential.

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TLDR
It is found that in cell lines containing inducible versions of alleles encoding the Pro72 and Arg72 variants, and in cells with endogenous p53, the Arg72 variant induces apoptosis markedly better than does the Pro 72 variant.
Abstract
The gene TP53, encoding p53, has a common sequence polymorphism that results in either proline or arginine at amino-acid position 72. This polymorphism occurs in the proline-rich domain of p53, which is necessary for the protein to fully induce apoptosis. We found that in cell lines containing inducible versions of alleles encoding the Pro72 and Arg72 variants, and in cells with endogenous p53, the Arg72 variant induces apoptosis markedly better than does the Pro72 variant. Our data indicate that at least one source of this enhanced apoptotic potential is the greater ability of the Arg72 variant to localize to the mitochondria; this localization is accompanied by release of cytochrome c into the cytosol. These data indicate that the two polymorphic variants of p53 are functionally distinct, and these differences may influence cancer risk or treatment.

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Citations
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Journal ArticleDOI

Influence of the TP53 codon 72 polymorphism on the cellular responses to X-irradiation in fibroblasts from nonagenarians

TL;DR: It is found that the average clonogenic survival after X-irradiation was similar for the three TP53 codon 72 genotype groups, and differences in cellular responses to stress between these genotypes contribute to the differences in cancer incidence and longevity observed earlier.
Journal ArticleDOI

Contribution of autophagic cell death to p53-dependent cell death in human glioblastoma cell line SF126

TL;DR: It is concluded that p53‐dependent cell death in SF126 cells comprises caspase‐dependent and caspases‐independent apoptosis and autophagic cell death, and the induction of autophagy as well as apoptosis could be a new strategy to treat some type of WT p53-retaining tumors.
Dissertation

ANÁLISE DO POLIMORFISMO DOS GENES TP53 E CYP1A1m1 EM BIÓPSIA DE ENDOMÉTRIO DE PACIENTES COM ENDOMETRIOSE

TL;DR: Fischer et al. as discussed by the authors evaluated the association between endometriose and polimorfismos of genes such as CYP1A1m1 and TP53.
Journal ArticleDOI

Functional nonsynonymous single nucleotide polymorphisms from the TGF-β protein interaction network

TL;DR: The naturally occurring human genetic variations that can affect the protein function and the TGF-beta signaling are analyzed and can be characterized by experimental approaches to elucidate their exact biological roles and whether they are related to human disease.
Journal ArticleDOI

Association of TP53 polymorphisms on the risk of Wilms tumor.

TL;DR: Molecular factors influencing Wilms tumor development remain largely unknown, but TP53 mutations seem to be restricted to the anaplastic WT subtype and TP53 polymorphisms do not have a defined role in the disease.
References
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Journal ArticleDOI

WAF1, a potential mediator of p53 tumor suppression

TL;DR: A gene is identified, named WAF1, whose induction was associated with wild-type but not mutant p53 gene expression in a human brain tumor cell line and that could be an important mediator of p53-dependent tumor growth suppression.
Journal ArticleDOI

Mice Lacking p21CIP1/WAF1 undergo normal development, but are defective in G1 checkpoint control

TL;DR: The results establish the role of p21CIP1/WAF1 in the G1 checkpoint, but suggest that the anti-apoptotic and theAnti-oncogenic effects of p53 are more complex.
Journal ArticleDOI

Protein regulation by monoubiquitin

TL;DR: Multi-ubiquitin chains at least four subunits long are required for efficient recognition and degradation of ubiquitylated proteins by the proteasome, but other functions of ubiquitin have been discovered that do not involve the protease.
Journal ArticleDOI

Role of a p53 polymorphism in the development of human papillomavirus-associated cancer.

TL;DR: Allelic analysis of patients with HPV-associated tumours revealed a striking overrepresentation of homozygous arginine-72 p53 compared with the normal population, which indicated that individuals homozygously for arginin 72 are about seven times more susceptible to HPV- associated tumorigenesis than heterozygotes.
Journal ArticleDOI

Death signal-induced localization of p53 protein to mitochondria. A potential role in apoptotic signaling

TL;DR: This work proposes a model where p53 can contribute to apoptosis by direct signaling at the mitochondria, thereby amplifying the transcription-dependent apoptosis of p53.
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